Term Name: infantile hypercalcemia 1
Synonyms:
Definition: A hypercalcemia that has_material_basis_in homozygous or compound heterozygous mutation in the CYP24A1 gene on chromosome 20q13.
Ontology: Human Disease [DOID:0061136]   ( DOID:0061136 )

Relationships
is a type of: autosomal recessive disease hypercalcemia inherited metabolic disorder